TY - JOUR
T1 - Microarray analysis of pneumococcal gene expression during invasive disease
AU - Orihuela, Carlos J.
AU - Radin, Jana N.
AU - Sublett, Jack E.
AU - Gao, Geli
AU - Kaushal, Deepak
AU - Tuomanen, Elaine I.
PY - 2004/10
Y1 - 2004/10
N2 - Streptococcus pneumoniae is a leading cause of invasive bacterial disease. This is the first study to examine the expression of S. pneumoniae genes in vivo by using whole-genome microarrays available from The Institute for Genomic Research. Total RNA was collected from pneumococci isolated from infected blood, infected cerebrospinal fluid, and bacteria attached to a pharyngeal epithelial cell line in vitro. Microarray analysis of pneumococcal genes expressed in these models identified body site-specific patterns of expression for virulence factors, transporters, transcription factors, translation-associated proteins, metabolism, and genes with unknown function. Contributions to virulence predicted for several unknown genes with enhanced expression in vivo were confirmed by insertion duplication mutagenesis and challenge of mice with the mutants. Finally, we cross-referenced our results with previous studies that used signature-tagged mutagenesis and differential fluorescence induction to identify genes that are potentially required by a broad range of pneumococcal strains for invasive disease.
AB - Streptococcus pneumoniae is a leading cause of invasive bacterial disease. This is the first study to examine the expression of S. pneumoniae genes in vivo by using whole-genome microarrays available from The Institute for Genomic Research. Total RNA was collected from pneumococci isolated from infected blood, infected cerebrospinal fluid, and bacteria attached to a pharyngeal epithelial cell line in vitro. Microarray analysis of pneumococcal genes expressed in these models identified body site-specific patterns of expression for virulence factors, transporters, transcription factors, translation-associated proteins, metabolism, and genes with unknown function. Contributions to virulence predicted for several unknown genes with enhanced expression in vivo were confirmed by insertion duplication mutagenesis and challenge of mice with the mutants. Finally, we cross-referenced our results with previous studies that used signature-tagged mutagenesis and differential fluorescence induction to identify genes that are potentially required by a broad range of pneumococcal strains for invasive disease.
UR - http://www.scopus.com/inward/record.url?scp=4644274689&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=4644274689&partnerID=8YFLogxK
U2 - 10.1128/IAI.72.10.5582-5596.2004
DO - 10.1128/IAI.72.10.5582-5596.2004
M3 - Article
C2 - 15385455
AN - SCOPUS:4644274689
SN - 0019-9567
VL - 72
SP - 5582
EP - 5596
JO - Infection and Immunity
JF - Infection and Immunity
IS - 10
ER -